Primary Site >> Stomach Cancer
Gene >> GPR35
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000319838 |
| Start | 240630473:240630473(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.521C>T |
| AA Mutation | p.Ala174Val(p.A174V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000319838 |
| Start | 240630209:240630209(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs527604027 |
| CDS Mutation | c.257C>T |
| AA Mutation | p.Thr86Met(p.T86M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000319838 |
| Start | 240630307:240630307(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199596106 |
| CDS Mutation | c.355C>T |
| AA Mutation | p.Arg119Trp(p.R119W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000319838 |
| Start | 240630008:240630008(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.56T>A |
| AA Mutation | p.Ile19Asn(p.I19N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000319838 |
| Start | 240630868:240630868(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs760148943 |
| CDS Mutation | c.916G>A |
| AA Mutation | p.Val306Met(p.V306M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000319838 |
| Start | 240630474:240630474(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs757134395 |
| CDS Mutation | c.522G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000319838 |
| Start | 240630036:240630036(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.84C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000319838 |
| Start | 240630546:240630546(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.594G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000319838 |
| Start | 240630363:240630363(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs745453974 |
| CDS Mutation | c.411C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |